Canonical Allele Identifier: CA406013471

Gene: BCKDHA

Linked Data

• MyVariant Identifiers: chr19:g.41928640G>T (hg19) ; chr19:g.41422735G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41422735G>T , CM000681.2:g.41422735G>T	GRCh38
NC_000019.9:g.41928640G>T , CM000681.1:g.41928640G>T	GRCh37
NC_000019.8:g.46620480G>T	NCBI36
NG_013004.1:g.29947G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269980.7:c.960G>T MANE Select	ENSP00000269980.2:p.Glu320Asp
ENST00000269980.6:c.960G>T	ENSP00000269980.2:p.Glu320Asp
ENST00000457836.6:c.894G>T	ENSP00000416000.2:p.Glu298Asp
ENST00000535632.5:n.589G>T
ENST00000540732.3:c.1062G>T	ENSP00000443246.1:p.Glu354Asp
ENST00000542943.5:c.873G>T	ENSP00000440345.1:p.Glu291Asp
ENST00000595085.5:c.922+38G>T	ENSP00000471150.2:n.922+38G>T
NM_000709.3:c.960G>T	NP_000700.1:p.Glu320Asp
NM_001164783.1:c.957G>T	NP_001158255.1:p.Glu319Asp
NM_000709.4:c.960G>T MANE Select	NP_000700.1:p.Glu320Asp
NM_001164783.2:c.957G>T	NP_001158255.1:p.Glu319Asp